Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.

Antzeko izenburuak

• Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features
  nork: Proks, P, et al.
  Argitaratua: (2005)
• Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.
  nork: Proks, P, et al.
  Argitaratua: (2004)
• Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions.
  nork: Tammaro, P, et al.
  Argitaratua: (2005)
• Focus on Kir6.2: a key component of the ATP-sensitive potassium channel.
  nork: Haider, S, et al.
  Argitaratua: (2005)
• Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.
  nork: Flanagan, SE, et al.
  Argitaratua: (2006)